Canonical Allele Identifier: PA2827921349
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774498
ClinVar RCV Id: RCV003592380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.His118Pro
CA352156956
NM_001354701.2:c.353A>C